Number of Panel Genes: 
21

Microcephalic primordial dwarfism consists of a group disorders including Meier-Gorlin syndrome, microcephalic osteodysplastic primordial dwarfism and Seckel syndrome. The main findings include intrauterine and postnatal growth retardation, severe short stature, and microcephaly. Microcephalic primordial dwarfism is caused by mutations in the genes involved in cell cycle and DNA repair.

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Tests Available

21 Panel Genes: ATR, ATRIP, CDC45, CDC6, CDT1, CENPJ, CEP63, CEP152, DNA2, DONSON, GMNN, LIG4, NIN, ORC1, ORC4, ORC6, PCNT, RBBP8, RNU4ATAC, TRAIP, XRCC4
Next Generation Sequencing
$1,420
Test Code: 5166
Deletion / Duplication
$990
Test Code: 5167
NGS/Del Dup Comprehensive
$1,795
Test Code: 5168

Test Details

Technical Information
Panel Genes: 
ATR, ATRIP, CDC45, CDC6, CDT1, CENPJ, CEP63, CEP152, DNA2, DONSON, GMNN, LIG4, NIN, ORC1, ORC4, ORC6, PCNT, RBBP8, RNU4ATAC, TRAIP, XRCC4
Disease Groups: 
Craniosynostosis and Craniofacial Disorders
Skeletal Dysplasias
Billing
Price: 
$1,420
CPT Codes: 
81479 x 21
Ordering
SKU:
5166
Turnaround Time: 
Typically 3 to 4 weeks from receipt of a sample in the laboratory. All cases involving ongoing pregnancies will be expedited.
Non-Prenatal Specimens: 
  1. Whole blood: purple-top (EDTA) tube, minimum of 3 ml
  2. Genomic DNA: minimum of 10 µg (at a concentration of at least 50 ng/µl)
  3. Fibroblasts: 4 confluent T-25 flasks
  4. Saliva: only samples collected in Oragene DNA Self-Collection Kit or Oragene Saliva Collection Kit for Young Children are accepted
Prenatal Specimens: 
  1. Cultured cells: 4 confluent T-25 flasks derived from amnio or CVS samples
  2. Genomic DNA: minimum of 10 µg (at a concentration of at least 50 ng/µl)
Shipping: 
Ship all specimen types at room temperature by overnight courier. Do not freeze.

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